Cerapedics, Inc.

FDA Device Registration & Listing · Westminster, CO, US · Registration 3007155473

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007155473
FEI Number
3007155473
Entity Name
Cerapedics, Inc.
City/State/Country
Westminster, CO, US
Establishment Address
11025 Dover Street, Suite 1600, Westminster, CO 80021, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Cerapedics, Inc. (Owner Number: 10026681)
Owner / Operator Contact Address
11025 Dover Street, Suite 1600, Westminster, CO 80021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P140019

All Registered Proprietary Names

PearlMatrix™ Peptide Enhanced Bone Graft i-FACTOR Peptide Enhanced Bone Graft

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NOX Filler, Bone Void, Synthetic Peptide Unknown Class 3 N/A 2025-07-01
NOX Filler, Bone Void, Synthetic Peptide Unknown Class 3 N/A 2015-12-16

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cerapedics, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007155473. Last updated year: 2026. Please use registration number 3007155473 when referencing this establishment in official correspondence.
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